戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 731225作成日:2026年10月26日

Water → 2-Benzylamino-5-nitro-benzenesulfonamide

https://huagongshe.com/reaction/731225

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物BenzylamineHCID 7504—
反応物2-Chloro-5-nitrobenzenesulfonamideHCID 66784—
反応物DiisopropylethylamineHCID 81531—
溶媒AcetonitrileHCID 6342—
生成物2-Benzylamino-5-nitro-benzenesulfonamideHCID 2485839783.4%

反応条件

温度55 °C

反応手順

A solution of 2-chloro-5-nitro-benzenesulfonamide (20 g, 84.52 mmol) in acetonitrile (169 mL) was treated with benzylamine (13.85 mL, 126.78 mmol), diisopropyl ethylamine (29.44 mL, 169.04 mmol) and stirred for 16 h at 55° C. The reaction was cooled to 25° C., poured into water (1.0 L) then placed in an ice bath while stirring. After 4 h a precipitate was filtered off and washed with the mother liquor to afford the desired product, 2-benzylamino-5-nitro-benzenesulfonamide (21.65 g, 70.45 mmol, 83.3%) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ: 4.64 (2H, d, J=4.6 Hz), 6.81 (1H, d, J=9.4 Hz), 7.23-7.44 (6H, m), 7.77 (2H, bs), 8.11 (1H, dd, J1=9.4 Hz, J2=2.3 Hz), 8.49 (1H, d, J=3.1 Hz). LC-MS (ESI) calcd for C13H13N3O4S 307.06, found 308.2 [M+H+] (100%), 615.2 [2M+H+] (81%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07582626B2
出典データセットuspto-grants-2009_09
ORD IDord-7471437e19c74501b00ff0a0c15570ab
出典メモuspto-grants-2009_09